1,4-Naphthalenedione,2-bromo-

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Names

[ CAS No. ]:
2065-37-4

[ Name ]:
1,4-Naphthalenedione,2-bromo-

[Synonym ]:
MFCD00629301
2-bromo-1,4-naphtoquinone
2-bromonaphthoquinone
3-Bromo-1,4-naphthoquinone
2-bromo-naphthalene-1,4-dione
2-Bromo-1,4-naphthoquinone

Chemical & Physical Properties

[ Density]:
1.757g/cm3

[ Boiling Point ]:
324.2ºC at 760mmHg

[ Melting Point ]:
131-133ºC(lit.)

[ Molecular Formula ]:
C10H5BrO2

[ Molecular Weight ]:
237.04900

[ Flash Point ]:
124.7ºC

[ Exact Mass ]:
235.94700

[ PSA ]:
34.14000

[ LogP ]:
2.34440

[ Vapour Pressure ]:
0.00025mmHg at 25°C

[ Index of Refraction ]:
1.674

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2914700090

Customs

[ HS Code ]: 2914700090

[ Summary ]:
HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

Articles

Potent naphthoquinones against antimony-sensitive and -resistant Leishmania parasites: synthesis of novel α- and nor-α-lapachone-based 1,2,3-triazoles by copper-catalyzed azide-alkyne cycloaddition.

Eur. J. Med. Chem. 63 , 523-30, (2013)

Continuing our screening program for novel anti-parasite compounds, we synthesized seven 1,4-naphthoquinones coupled to 1,2,3-triazoles, five nor-β-lapachone-based 1,2,3-triazoles and ten α-lapachone-...

2-Bromo-1,4-naphthoquinone: a potentially improved substitute of menadione in Apatone™ therapy.

Braz. J. Med. Biol. Res. 45(8) , 701-10, (2012)

Apatone™, a combination of menadione (2-methyl-1,4-naphthoquinone, VK3) and ascorbic acid (vitamin C, VC) is a new strategy for cancer treatment. Part of its effect on tumor cells is related to the ce...

Expedient, one-pot preparation of fused indoles via CAN-catalyzed three-component domino sequences and their transformation into polyheterocyclic compounds containing pyrrolo[1,2-a]azepine fragments.

Org. Biomol. Chem. 8(15) , 3426-36, (2010)

The CAN-catalyzed three-component between reaction between primary amines, beta-dicarbonyl compounds and naphthoquinones or 2-bromonaphthoquinones afforded, respectively, 5-hydroxybenzo[g]indoles and ...


More Articles


Related Compounds

  • 1,4-Naphthalenedione,2-bromo-3-ethyl
  • 1,4-Naphthalenedione,2-bromo-3-butyl
  • 1,4-Naphthalenedione,2-bromo-3-chloro
  • 1,4-Naphthalenedione,2-bromo-8-methyl
  • 1,4-Naphthalenedione,2-bromo-3-ethoxy
  • 1,4-Naphthalenedione,2-bromo-3-heptyl
  • N-butyl-3-methoxypropanehydrazide
  • 2-(azetidin-3-yloxy)-5-chloro-1H-indole
  • 3-[6-(Aminomethyl)piperidin-3-yl]benzaldehyde
  • 2,2-Diethyl-6-(iodomethyl)-1,4-dioxane
  • 1-(hexa-3,5-dien-1-yl)-1H-pyrazol-4-amine
  • 1-[(2,4-Dimethyl-1,3-thiazol-5-yl)methyl]-3-fluoropyrrolidine-3-carboxamide
  • 1-(6-Chloro-1,3-benzothiazol-2-yl)piperidine-4-carboxamide
  • 4-[2-(Difluoromethoxy)-3-methylphenyl]-1,3-oxazolidin-2-one
  • 1-(Benzyloxy)-3-(methoxy-d3)-5-(trifluoromethoxy)benzene
  • 4,4-Difluoro-1-(5-methoxypyridin-3-yl)cyclohexane-1-carboxylic acid
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